Canonical Allele Identifier: CA2038922546
Gene: KIF5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57567914_57567916delinsGCT , CM000674.2:g.57567914_57567916delinsGCT GRCh38
NC_000012.11:g.57961697_57961699delinsGCT , CM000674.1:g.57961697_57961699delinsGCT GRCh37
NC_000012.10:g.56247964_56247966delinsGCT NCBI36
NG_008155.1:g.22851_22853delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.714+296_714+298delinsGCT MANE Select ENSP00000408979.2:n.714+296_714+298delinsGCT
ENST00000674619.1:c.714+296_714+298delinsGCT ENSP00000502270.1:n.714+296_714+298delinsGCT
ENST00000676457.1:c.609+296_609+298delinsGCT ENSP00000501588.1:n.609+296_609+298delinsGCT
ENST00000286452.5:c.447+296_447+298delinsGCT ENSP00000286452.5:n.447+296_447+298delinsGCT
ENST00000455537.6:c.714+296_714+298delinsGCT ENSP00000408979.2:n.714+296_714+298delinsGCT
NM_004984.2:c.714+296_714+298delinsGCT NP_004975.2:n.714+296_714+298delinsGCT
NM_001354705.1:c.447+296_447+298delinsGCT NP_001341634.1:n.447+296_447+298delinsGCT
NM_004984.3:c.714+296_714+298delinsGCT NP_004975.2:n.714+296_714+298delinsGCT
XR_002957324.1:n.947+296_947+298delinsGCT
NM_004984.4:c.714+296_714+298delinsGCT MANE Select NP_004975.2:n.714+296_714+298delinsGCT
NM_001354705.2:c.447+296_447+298delinsGCT NP_001341634.1:n.447+296_447+298delinsGCT